Search results for bdnf

1130 hits were found for bdnf

# Family MCID Name MIFTS Score
1
DPR016 Depression 65 23.104
2
P MJR001 Major Depressive Disorder 68 22.405
3
P BPL003 Bipolar Disorder 56 21.309
4
CNT097 Central Hypoventilation Syndrome, Congenital 70 20.862
5
P SCH015 Schizophrenia 74 19.386
6
P HNT016 Huntington Disease 73 18.712
7
MNT002 Mental Depression 56 18.010
8
ANX010 Anxiety 70 17.916
9
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 53 17.895
10
MDD011 Mood Disorder 62 17.852
11
P ALZ034 Alzheimer Disease 87 15.725
12
ISC004 Ischemia 61 14.903
13
P RTT002 Rett Syndrome 79 14.832
14
ETN001 Eating Disorder 59 14.829
15
SPN186 Spinal Cord Injury 61 14.708
16
P EPL164 Epilepsy 70 14.550
17
P NRB001 Neuroblastoma 66 14.541
18
P DMN002 Dementia 65 14.462
19
PST028 Post-Traumatic Stress Disorder 59 13.719
20
P MLT020 Multiple Sclerosis 79 13.589
21
P ATS364 Autism 72 13.581
22
CRB004 Cerebral Artery Occlusion 46 13.554
23
P ATT013 Attention Deficit-Hyperactivity Disorder 66 13.511
24
P PRK057 Parkinson Disease, Late-Onset 79 13.228
25
PSY004 Psychotic Disorder 66 13.200
26
c AMY091 Amyotrophic Lateral Sclerosis 1 88 12.900
27
OBS002 Obsessive-Compulsive Disorder 68 12.855
28
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 12.769
29
P BRS047 Breast Cancer 97 12.695
30
STT001 Status Epilepticus 58 12.671
31
ALC007 Alcohol Dependence 65 12.607
32
ANR007 Anorexia Nervosa 59 12.602
33
P TMP001 Temporal Lobe Epilepsy 49 12.572
34
BLM002 Bulimia Nervosa 57 11.944
35
P ALC033 Alcohol Use Disorder 67 11.858
36
P AST005 Asthma 76 11.799
37
c ATS007 Autism Spectrum Disorder 72 11.613
38
STR067 Stroke, Ischemic 79 11.450
39
RLP002 Relapsing-Remitting Multiple Sclerosis 56 11.419
40
P SNS001 Sensorineural Hearing Loss 59 11.338
41
SCH012 Schizoaffective Disorder 49 11.263
42
P HRT032 Heart Disease 84 11.084
43
P MTR014 Motor Neuron Disease 65 11.080
44
TRM010 Traumatic Brain Injury 50 10.848
45
P PNC025 Panic Disorder 52 10.802
46
BRN071 Brain Injury 50 10.688
47
MLD018 Mild Cognitive Impairment 48 10.612
48
P PRS038 Personality Disorder 65 10.512
49
c TYP009 Type 2 Diabetes Mellitus 92 10.450
50
FBR047 Fibromyalgia 58 10.396
51
SDD001 Sudden Infant Death Syndrome 60 10.250
52
P SBS003 Substance Abuse 54 10.230
53
IRR002 Irritable Bowel Syndrome 65 10.136
54
P DBT009 Diabetes Mellitus 67 10.084
55
P RTN016 Retinal Degeneration 52 9.990
56
ACT084 Acute Stress Disorder 53 9.865
57
P ANR048 Aniridia 1 66 9.782
58
GNR004 Generalized Anxiety Disorder 55 9.666
59
c BPL002 Bipolar I Disorder 47 9.661
60
P NRP001 Neuropathy 59 9.624
61
BRD004 Borderline Personality Disorder 53 9.599
62
c MJR024 Major Affective Disorder 9 40 9.562
63
c MJR022 Major Affective Disorder 8 37 9.562
64
PST021 Postpartum Depression 50 9.484
65
P FRG001 Fragile X Syndrome 70 9.439
66
PRN009 Paranoid Schizophrenia 49 9.298
67
APH002 Aphasia 55 9.291
68
CRB037 Cerebral Palsy 67 9.256
69
P OPN001 Open-Angle Glaucoma 55 9.230
70
P DRM053 Dermatitis, Atopic 65 9.219
71
CRT072 Creutzfeldt-Jakob Disease 67 9.214
72
P CRD246 Cardiovascular System Disease 55 9.156
73
P SLP006 Sleep Apnea 69 9.150
74
P DYS154 Dystonia 64 9.129
75
HRN003 Heroin Dependence 44 9.105
76
FTL006 Fetal Alcohol Spectrum Disorder 43 9.087
77
P CYS018 Cystitis 59 9.080
78
CNS004 Constipation 56 9.072
79
CCN001 Cocaine Dependence 48 8.835
80
c CNT035 Central Nervous System Disease 53 8.713
81
DRG003 Drug Dependence 46 8.687
82
P INT143 Interstitial Cystitis 59 8.646
83
CRV043 Cervical Dystonia 45 8.642
84
CCN002 Cocaine Abuse 49 8.636
85
P EYD002 Eye Disease 57 8.608
87
GLL008 Gilles De La Tourette Syndrome 64 8.567
88
NRT004 Neuritis 53 8.563
89
P MDL005 Medulloblastoma 75 8.425
90
P HYD006 Hydrocephalus 63 8.425
91
P BLP003 Blepharospasm 45 8.410
92
P OST002 Osteoporosis 77 8.356
93
LPT014 Leptin Deficiency or Dysfunction 77 8.345
94
END040 Endogenous Depression 54 8.341
95
P NRC002 Narcolepsy 55 8.329
96
c WLM013 Wilms Tumor 1 65 8.309
97
P PRD006 Prader-Willi Syndrome 60 8.261
98
SBS004 Substance Dependence 46 8.207
99
c ESS001 Essential Tremor 56 8.183
100
P OPT009 Optic Neuritis 57 8.183
101
P NRM002 Normal Pressure Hydrocephalus 49 8.171
102
CNN002 Cannabis Abuse 44 8.171
103
TRN012 Transient Global Amnesia 38 8.100
104
TBC004 Tobacco Addiction 63 8.057
105
SKN016 Skin Disease 62 8.021
106
BNG009 Benign Epilepsy with Centrotemporal Spikes 60 8.004
107
AMN003 Amnestic Disorder 54 7.996
108
SNS003 Sensory Peripheral Neuropathy 51 7.804
109
NTR005 Nutritional Deficiency Disease 60 7.772
110
c SCN036 Secondary Progressive Multiple Sclerosis 55 7.737
111
CHR066 Chronic Fatigue Syndrome 60 7.724
112
CRT015 Carotid Artery Occlusion 45 7.714
113
c PRM108 Primary Progressive Multiple Sclerosis 51 7.669
114
MNN009 Meningoencephalitis 48 7.669
115
P ASP001 Asperger Syndrome 48 7.653
116
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 7.558
117
SGM008 Segmental Dystonia 28 7.532
118
P PRP019 Peripheral Nervous System Disease 57 7.508
119
DRY001 Dry Eye Syndrome 49 7.462
120
P HRD021 Hereditary Sensory Neuropathy 48 7.462
121
P SLP005 Sleep Disorder 62 7.454
122
c HYP595 Hypertension, Essential 84 7.367
123
SPC010 Speech and Communication Disorders 48 7.367
124
c MGR028 Migraine with or Without Aura 1 64 7.233
125
OCL052 Ocular Dominance 40 7.224
126
P OPT006 Optic Nerve Disease 57 7.088
127
P FTL001 Fetal Alcohol Syndrome 55 7.009
128
P MVM001 Movement Disease 61 6.971
129
c GLC092 Glaucoma, Primary Open Angle 61 6.945
130
DSS008 Disease of Mental Health 74 6.857
131
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 36 6.829
132
NRM005 Neuromuscular Disease 63 6.796
133
SCH003 Schizophreniform Disorder 54 6.776
134
PNG002 Pain Agnosia 51 6.716
135
RTN003 Retinal Ischemia 48 6.703
136
P RTN008 Retinitis Pigmentosa 79 6.671
137
ADR040 Adrenal Gland Pheochromocytoma 45 6.645
138
MYF002 Myofascial Pain Syndrome 46 6.641
139
c EXD008 Exudative Vitreoretinopathy 1 71 6.547
140
c PNS012 Paine Syndrome 60 6.484
141
NRG002 Neurogenic Bladder 55 6.459
142
NRT001 Neurotic Disorder 56 6.457
143
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 6.430
144
DYS009 Dysthymic Disorder 51 6.421
145
CNV002 Conversion Disorder 47 6.337
146
c ERL020 Early-Onset Schizophrenia 43 6.308
147
TRG002 Trigeminal Neuralgia 61 6.299
148
AMB002 Amblyopia 49 6.288
149
SCL003 Social Phobia 48 6.246
150
TND006 Tendinosis 40 6.223
151
DBT081 Diabetic Encephalopathy 36 6.187
152
SXL003 Sexual Disorder 49 6.143
153
MLN003 Melancholia 41 6.072
154
ADJ001 Adjustment Disorder 46 6.038
155
SBJ001 Subjective Cognitive Decline 30 5.986
156
PCK003 Pick Disease of Brain 69 5.972
157
ATY001 Atypical Depressive Disorder 45 5.972
158
SMT006 Somatoform Disorder 50 5.942
159
ASP004 Asphyxia Neonatorum 50 5.926
160
P PRV006 Pervasive Developmental Disorder 52 5.908
161
PHB001 Phobic Disorder 45 5.869
162
P CHR345 Chronic Pain 50 5.811
163
RTR001 Retrograde Amnesia 41 5.791
164
P NRV007 Nervous System Disease 66 5.705
165
CHR073 Choreatic Disease 53 5.686
166
CHL012 Childhood Disintegrative Disease 44 5.511
167
DMN031 Dementia, Lewy Body 65 5.462
168
FND002 Fundus Dystrophy 55 5.423
169
WRN002 Wernicke-Korsakoff Syndrome 49 5.400
170
ANT019 Anterograde Amnesia 38 5.400
171
HYL004 Hyaline Fibromatosis Syndrome 66 5.209
172
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 5.209
173
LBS001 Lubs X-Linked Mental Retardation Syndrome 49 5.209
174
KGM001 Kagami-Ogata Syndrome 54 5.209
175
c NRP037 Neuropathy, Hereditary Sensory and Autonomic, Type V 55 5.209
176
c DFN257 Deafness, Autosomal Dominant 33 21 5.209
177
XLN230 X-Linked Monogenic Disease 17 5.209
178
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 5.209
179
KFM001 Kaufman Oculocerebrofacial Syndrome 55 5.209
180
CRT007 Cortical Deafness 26 5.209
181
c ATM007 Autoimmune Disease of Central Nervous System 30 5.209
182
SPC003 Specific Developmental Disorder 31 5.209
183
CHR569 Chromosomal Duplication Syndrome 21 5.209
184
PHB003 Phobia, Specific 44 5.209
185
c NNN021 Noonan Syndrome 8 39 5.209
186
c AML044 Amelogenesis Imperfecta, Type Ig 53 5.209
187
P TTR001 Tetralogy of Fallot 69 5.209
188
DSS010 Dissociative Disorder 39 5.209
189
ENC005 Encephalomalacia 43 5.209
190
P CHR084 Chromosomal Disease 34 5.209
191
GND018 Gene Duplication Disease 23 5.209
192
STR007 Stress Polycythemia 26 5.209
193
OCC005 Occlusion Precerebral Artery 28 5.209
194
TRG003 Trigeminal Nerve Disease 37 5.209
195
CRN031 Cranial Nerve Disease 37 5.209
196
NRV002 Nerve Fibre Bundle Defect 10 5.209
197
P ATN003 Autonomic Nervous System Neoplasm 25 5.209
198
HYP016 Hypochondriasis 47 5.209
199
P PRP021 Peripheral Nervous System Neoplasm 37 5.209
200
SXL001 Sexual Sadism 31 5.209
201
P AGN002 Agnosia 53 5.209
202
c ATM017 Autoimmune Disease of the Nervous System 37 5.209
203
TXC002 Toxic Encephalopathy 51 5.209
204
P AML002 Amelogenesis Imperfecta 56 5.209
205
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 61 5.209
206
THM026 Thiamine Deficiency Disease 24 5.209
207
AGN016 Aging 54 5.013
208
HYP266 Hypoxia 56 4.797
209
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 3.925
210
P SZR006 Seizure Disorder 69 3.922
211
P LTR001 Lateral Sclerosis 58 3.878
212
HYP066 Hyperglycemia 60 3.733
213
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.389
214
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 3.389
215
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.389
216
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.389
217
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 3.389
218
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.389
219
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.389
220
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.389
221
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 3.389
222
ALL029 Allergic Disease 61 3.231
223
VSC002 Vascular Dementia 59 3.169
224
CYT002 Cytokine Deficiency 43 3.164
225
c BRN108 Branchiootic Syndrome 1 63 2.989
226
INT323 Intraocular Pressure Quantitative Trait Locus 63 2.940
227
GLM045 Glioma 62 2.929
228
SVR004 Severe Combined Immunodeficiency 71 2.894
229
GLL048 Glial Tumor 52 2.855
230
P SMK004 Smoking As a Quantitative Trait Locus 3 44 2.848
231
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.817
232
P BCL017 B-Cell Lymphoma 57 2.791
233
P MJR007 Major Affective Disorder 1 42 2.752
234
CRB039 Cerebrovascular Disease 65 2.745
235
ALL014 Allergic Encephalomyelitis 34 2.733
236
c MCR115 Microvascular Complications of Diabetes 5 65 2.671
237
P CRN300 Coronary Heart Disease 1 73 2.650
238
ALL006 Allergic Asthma 56 2.594
239
TTN003 Tetanus 64 2.505
240
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.488
241
P END044 Endometriosis 62 2.384
242
P ENC018 Encephalopathy 62 2.371
243
MYL069 Myeloma, Multiple 77 2.304
244
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 2.264
245
IMP005 Impotence 52 2.223
246
P MNN013 Meningitis 65 2.187
247
DBT010 Diabetic Neuropathy 54 2.183
248
P MYC007 Myocardial Infarction 69 2.153
249
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.066
250
DRM006 Dermatitis 62 2.048
251
OCL006 Ocular Hypertension 53 2.044
252
P PRK039 Parkinsonism 55 2.040
253
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.034
254
48X005 48,xyyy 39 2.031
255
OPT003 Opiate Dependence 49 1.974
256
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.953
257
HYP060 Hyperinsulinism 53 1.948
258
INS024 Insulin-Like Growth Factor I 77 1.943
259
GLC003 Glucose Intolerance 53 1.921
260
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.920
261
SQM006 Squamous Cell Carcinoma 59 1.920
262
c BCT007 Bacterial Meningitis 55 1.892
263
BRN004 Brain Edema 54 1.887
264
HDN002 Head Injury 44 1.884
265
AVD001 Avoidant Personality Disorder 49 1.880
266
DWN001 Down Syndrome 70 1.875
267
GLB002 Glioblastoma 67 1.820
268
WTH001 Withdrawal Disorder 47 1.814
269
SPS057 Spasticity 43 1.808
270
TRD006 Tardive Dyskinesia 53 1.783
271
VCC001 Vaccinia 49 1.780
272
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 17 1.773
273
ART140 Arteries, Anomalies of 52 1.750
274
LPP008 Lipoprotein Quantitative Trait Locus 65 1.750
275
OPD006 Opioid Addiction 48 1.750
276
CRV035 Cervical Cancer 72 1.748
277
HYP056 Hypoglycemia 65 1.738
278
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.731
279
P HYP086 Hypothyroidism 69 1.731
280
DYS073 Dysphagia 53 1.720
281
TRN015 Transient Cerebral Ischemia 62 1.714
282
LPD008 Lipid Metabolism Disorder 61 1.699
283
P CLR023 Colorectal Cancer 100 1.690
284
FCL014 Focal Epilepsy 53 1.660
285
PST011 Pustulosis of Palm and Sole 52 1.646
286
P PSR002 Psoriasis 63 1.646
287
P RTN018 Retinal Disease 53 1.639
288
c SML038 Small Cell Cancer of the Lung 69 1.632
289
HLX001 Helix Syndrome 47 1.610
290
ATH013 Atherosclerosis Susceptibility 63 1.610
291
P GLM040 Glioma Susceptibility 1 70 1.588
292
MRP001 Morphine Dependence 41 1.587
293
MLG169 Malignant Astrocytoma 57 1.561
294
SBC016 Subacute Delirium 42 1.557
295
P RHN004 Rhinitis 57 1.537
296
P CRD119 Cardiac Arrest 68 1.531
297
CNG034 Congestive Heart Failure 69 1.525
298
CHL014 Cholera 62 1.513
299
ALL003 Allergic Rhinitis 66 1.500
300
P MSC003 Muscular Atrophy 52 1.497
301
CLT003 Colitis 63 1.494
302
P ENC004 Encephalitis 61 1.489
303
IRN002 Iron Metabolism Disease 56 1.488
304
P INF032 Infertility 60 1.475
305
c MJR006 Major Affective Disorder 5 32 1.460
306
c MJR003 Major Affective Disorder 6 32 1.460
307
47X002 47,xyy 48 1.455
308
P BLD134 Bladder Cancer 79 1.442
309
c SCH079 Schizophrenia 1 44 1.441
310
P TRM003 Tremor 50 1.441
311
P PHC003 Pheochromocytoma 70 1.436
312
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.433
313
c CHR684 Chronic Kidney Disease 74 1.421
314
c PRC016 Pre-Eclampsia 64 1.419
315
DMY004 Demyelinating Disease 50 1.419
316
P VSC007 Vascular Disease 62 1.414
317
ATN005 Autonomic Dysfunction 45 1.414
318
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.395
319
P RTN024 Retinoblastoma 72 1.392
320
FRN006 Frontotemporal Dementia 68 1.392
321
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.392
322
P BNC003 Bone Cancer 58 1.389
323
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.380
324
P CRB088 Cerebral Atrophy 33 1.377
325
P OVR082 Overgrowth Syndrome 42 1.370
326
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 1.370
327
P PLY019 Polyneuropathy 53 1.370
328
c SYS001 Systemic Lupus Erythematosus 86 1.365
329
P LPS004 Lupus Erythematosus 61 1.365
330
OCL069 Ocular Motor Apraxia 57 1.358
332
P GST053 Gastric Cancer 82 1.346
333
OST159 Osteogenic Sarcoma 66 1.341
334
P KDN018 Kidney Disease 72 1.322
335
PNM013 Pneumococcal Meningitis 43 1.293
336
P OVR042 Ovarian Cancer 88 1.287
337
P HDC001 Headache 56 1.286
338
LWC001 Low Compliance Bladder 44 1.284
339
INT007 Intermediate Coronary Syndrome 53 1.279
340
NRR001 Neuroretinitis 42 1.272
341
AMN001 Amenorrhea 53 1.272
342
RTN023 Retinitis 45 1.272
343
CHR178 Chromosomal Triplication 34 1.269
344
OST012 Osteoarthritis 77 1.257
345
HGH043 High Grade Glioma 46 1.251
346
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 1.243
347
PPL052 Papillomatosis, Confluent and Reticulated 34 1.241
348
c ACT075 Acute Myocardial Infarction 55 1.241
349
LRN003 Learning Disability 49 1.241
350
P PNC035 Pancreatic Cancer 86 1.231
351
P AMY004 Amyloidosis 69 1.221
352
P PLM037 Pulmonary Hypertension 69 1.220
353
c MCR112 Microvascular Complications of Diabetes 2 42 1.212
354
P MCR129 Microvascular Complications of Diabetes 1 68 1.212
355
GST033 Gestational Diabetes 61 1.212
356
PRT037 Pertussis 49 1.200
357
P ART022 Arthritis 70 1.198
358
BNR002 Bone Resorption Disease 47 1.196
359
P PRD008 Periodontitis 64 1.196
360
P RST001 Restless Legs Syndrome 52 1.190
361
PLY150 Polykaryocytosis Inducer 29 1.171
362
PLY068 Polysubstance Abuse 41 1.163
363
P LNG032 Lung Cancer 98 1.163
364
FTT001 Fatty Liver Disease 61 1.163
365
MSC007 Muscle Hypertrophy 64 1.155
366
ATM095 Autoimmune Disease 61 1.154
367
HPT004 Hepatic Coma 43 1.137
368
HPT019 Hepatic Encephalopathy 59 1.137
369
PLC005 Placental Insufficiency 56 1.137
370
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 1.131
371
P MGL013 Megalencephaly 46 1.131
372
P BND020 Bone Disease 60 1.128
373
P PRS040 Prostate Cancer 95 1.118
374
P MPL001 Maple Syrup Urine Disease 69 1.118
375
c TYP008 Type 1 Diabetes Mellitus 77 1.118
376
P MYP004 Myopathy 67 1.118
377
ALX002 Alexithymia 37 1.118
378
P TCD001 Tic Disorder 50 1.118
379
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.109
380
THY029 Thyroid Carcinoma 54 1.104
381
DFC004 Deficiency Anemia 74 1.099
382
RST023 Resting Heart Rate, Variation in 40 1.099
383
ORL015 Oral Squamous Cell Carcinoma 43 1.089
384
END057 Endometrial Cancer 71 1.089
385
P HPT023 Hepatocellular Carcinoma 95 1.089
386
SCH011 Schizotypal Personality Disorder 36 1.079
387
SPP007 Suppression Amblyopia 38 1.079
388
P HYP750 Hypertriglyceridemia, Familial 62 1.079
389
P HRP006 Herpes Simplex 65 1.079
390
ANG054 Angina Pectoris 65 1.072
391
INS001 Insulinoma 59 1.069
392
P CHN012 Chondrosarcoma 56 1.065
393
ADN011 Adenoid Cystic Carcinoma 68 1.058
394
TRN018 Transitional Cell Carcinoma 56 1.058
395
P FBR031 Febrile Seizures 52 1.058
396
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.025
397
CND002 Conduct Disorder 50 1.025
398
ADN018 Adenoma 58 1.025
399
PTH003 Pathologic Nystagmus 52 1.025
400
HYP835 Hypothalamic Obesity 38 1.025
401
P LKM071 Leukemia, Chronic Lymphocytic 74 1.013
402
ACS001 Acoustic Neuroma 56 1.013
403
PTH002 Pathological Gambling 48 1.013
404
NRL005 Neurilemmoma 60 1.013
406
P RHM011 Rheumatoid Arthritis 81 1.006
407
PRX005 Peroxisomal Biogenesis Disorder 35 1.001
408
c SPN294 Spinocerebellar Ataxia 1 53 1.001
409
DPR002 Depersonalization Disorder 41 1.001
410
GST045 Gastroenteritis 58 1.001
411
END086 End Stage Renal Disease 54 1.001
412
c PCH010 Pachyonychia Congenita 3 43 0.989
413
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 0.989
414
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.989
415
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.989
416
TRN007 Transsexualism 38 0.989
417
SYN116 Syndromic Obesity 27 0.989
418
CMB007 Combined Immunodeficiency 56 0.978
419
APN008 Apnea, Obstructive Sleep 66 0.978
420
P DRR001 Diarrhea 55 0.976
421
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.976
422
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.967
423
c SPN309 Spinocerebellar Ataxia 6 58 0.962
424
PRP016 Paraplegia 52 0.962
425
P INF037 Inflammatory Bowel Disease 53 0.961
426
LNG039 Lung Squamous Cell Carcinoma 57 0.961
427
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.952
428
P PLY011 Polycystic Ovary Syndrome 57 0.952
429
BCK006 Back Pain 43 0.952
430
HYP679 Hypoglossia-Hypodactylia 33 0.948
431
c TYR013 Tyrosinemia, Type Ii 48 0.948
432
HMS001 Hemosiderosis 48 0.948
433
P TYR004 Tyrosinemia 49 0.948
434
LRY022 Laryngoonychocutaneous Syndrome 43 0.943
435
PRM020 Premenstrual Tension 39 0.943
436
P TRN020 Turner Syndrome 67 0.940
437
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.933
438
THR024 Thrombosis 56 0.933
439
P ANP001 Anaplastic Large Cell Lymphoma 61 0.924
440
NRN001 Neuroendocrine Carcinoma 47 0.924
441
BRN018 Borna Disease 36 0.918
442
PRS129 Prostatic Hyperplasia, Benign 48 0.914
443
PRS021 Prostatic Adenoma 43 0.914
444
PRS045 Prostatic Hypertrophy 52 0.914
445
LVR012 Liver Cirrhosis 62 0.904
446
ORL011 Oral Cancer 60 0.902
447
c MCR133 Microvascular Complications of Diabetes 4 41 0.894
448
c MCR113 Microvascular Complications of Diabetes 3 52 0.894
449
c MCR130 Microvascular Complications of Diabetes 6 41 0.894
450
c MCR120 Microvascular Complications of Diabetes 7 47 0.894
451
P MGR003 Migraine with Aura 51 0.894
452
AGR002 Agoraphobia 45 0.894
453
CHR074 Choriocarcinoma 46 0.884
454
OPD001 Opioid Abuse 44 0.873
455
P MSC005 Muscular Dystrophy 66 0.873
456
SMT008 Smith-Magenis Syndrome 53 0.865
457
PRM013 Premature Menopause 57 0.863
458
c HYP836 Hypercholesterolemia, Familial, 1 73 0.863
459
ANX004 Anoxia 40 0.863
460
DGN001 Degenerative Disc Disease 48 0.863
461
RBS001 Rabies 58 0.852
462
NRM004 Neuroma 49 0.852
463
PHY002 Physical Disorder 41 0.852
464
c ACT073 Acute Leukemia 59 0.852
465
P MGR001 Migraine Without Aura 48 0.852
466
P PRN023 Prion Disease 60 0.852
467
P PNC044 Pancreatitis 61 0.852
468
BCK003 Background Diabetic Retinopathy 46 0.852
469
P ECL001 Eclampsia 52 0.852
470
MSC157 Muscular Dystrophy, Duchenne Type 79 0.852
471
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.852
472
P HYP263 Hypersomnia 40 0.845
473
IRN001 Iron Deficiency Anemia 58 0.828
474
P ATR011 Atrial Fibrillation 66 0.828
475
NRL016 Neural Tube Defects 81 0.816
476
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.816
477
OVR063 Overnutrition 42 0.816
478
DBT004 Diabetic Polyneuropathy 50 0.816
479
DBT002 Diabetic Autonomic Neuropathy 40 0.816
480
HMC014 Homocysteinemia 52 0.804
481
BLR008 Bilirubin Metabolic Disorder 57 0.804
482
PRT058 Pure Autonomic Failure 58 0.797
483
HMN044 Human Immunodeficiency Virus Type 1 76 0.793
484
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.791
485
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.791
486
PRV004 Periventricular Leukomalacia 52 0.791
487
P ADN016 Adenocarcinoma 63 0.791
488
BRN028 Brain Cancer 73 0.791
489
NNT024 Neonatal Stroke 31 0.791
490
FTL021 Fetal Macrosomia 40 0.791
491
ADL002 Adult Syndrome 69 0.789
492
RHB024 Rhabdomyosarcoma 2 65 0.789
493
c ATR087 Atrial Standstill 1 74 0.777
494
P LPR021 Leprosy 3 71 0.777
495
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.777
496
P LNG064 Lung Cancer Susceptibility 3 70 0.777
497
PLM038 Pulmonary Large Cell Neuroendocrine Carcinoma 31 0.777
498
c HPT016 Hepatitis B 62 0.777
499
P HPT021 Hepatitis 68 0.777
500
PLS011 Plasmacytoma 56 0.777
501
LSN001 Lesion of Sciatic Nerve 22 0.777
502
P CLS010 Cluster Headache 42 0.777
503
HNS001 Hansen's Disease 32 0.777
504
CHG001 Chagas Disease 65 0.767
505
BRN026 Branch Retinal Artery Occlusion 41 0.763
506
HYP008 Hypertensive Retinopathy 39 0.763
507
P LKM002 Leukemia 66 0.763
508
CRV038 Cervical Squamous Cell Carcinoma 56 0.763
509
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.763
510
P RTN014 Retinal Artery Occlusion 47 0.763
512
ISL011 Isolated Aniridia 37 0.763
513
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.748
514
P URN019 Urinary Tract Infection 49 0.748
515
CHL067 Cholecystitis 59 0.748
516
GLL017 Gallbladder Adenocarcinoma 42 0.748
517
CRT033 Corticobasal Degeneration 48 0.748
518
LKP003 Leukoplakia 39 0.748
519
SMN008 Semantic Dementia 47 0.748
520
SPN092 Spinal Shock 19 0.748
521
MNN024 Meningitis and Encephalitis 27 0.748
522
ORL012 Oral Leukoplakia 35 0.748
523
ACT119 Acute Promyelocytic Leukemia 62 0.733
524
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.733
525
AML029 Ameloblastoma 46 0.733
526
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.733
527
c OPT053 Optic Atrophy 1 62 0.733
528
c SCH087 Schizophrenia 18 28 0.733
529
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.733
530
P STR020 Strabismus 56 0.733
531
GND002 Gender Identity Disorder 40 0.733
532
NRN004 Neuroendocrine Tumor 55 0.733
533
P PLM036 Pulmonary Fibrosis 65 0.733
534
P KLL001 Kallmann Syndrome 65 0.733
535
PST047 Post-Traumatic Epilepsy 20 0.733
536
MCH006 Mechanical Strabismus 40 0.733
537
NRM001 Neuromyelitis Optica 60 0.733
538
ARG004 Argyria 26 0.733
539
PRM329 Premature Aging 36 0.733
540
IMM167 Immune Deficiency Disease 77 0.721
541
c NPH049 Nephrotic Syndrome, Type 2 52 0.717
542
PRT251 Proteinuria, Chronic Benign 58 0.717
543
NNL006 Non-Alcoholic Steatohepatitis 54 0.717
544
CLR109 Colorectal Adenocarcinoma 50 0.717
545
SCK003 Sickle Cell Anemia 74 0.717
546
HRW001 Hair Whorl 35 0.717
547
MNN017 Mononeuropathy 41 0.717
548
GNG002 Ganglioneuroma 52 0.717
549
HYP080 Hypogonadism 49 0.717
550
c NPH055 Nephrotic Syndrome, Type 1 52 0.717
551
c ERL012 Early-Onset Glaucoma 23 0.717
552
P DYS021 Dysautonomia 38 0.717
553
PDT048 Pediatric-Onset Glaucoma of Genetic Origin 11 0.717
554
PST053 Postherpetic Neuralgia 40 0.717
555
AML004 Ameloblastic Carcinoma 39 0.717
556
P CRB059 Cerebellar Degeneration 36 0.717
557
CHL078 Childhood-Onset Schizophrenia 29 0.717
558
c ATM075 Autoimmune Encephalitis 39 0.717
559
NRF007 Neurofibroma 64 0.717
560
P RRH023 Rare Hereditary Hemochromatosis 53 0.717
561
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.699
563
P HYP730 Hypogonadotropic Hypogonadism 54 0.699
564
c THR092 Thrombophilia Due to Thrombin Defect 74 0.699
565
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 0.699
566
P SPN046 Spinal Muscular Atrophy 62 0.699
567
P KDN017 Kidney Cancer 60 0.699
568
SMT001 Somatization Disorder 50 0.699
569
PRS047 Prostatitis 58 0.699
570
c DLT002 Dilated Cardiomyopathy 79 0.699
571
PCD001 Pica Disease 38 0.699
572
DPH001 Diphtheria 59 0.699
573
P PLY020 Polyradiculoneuropathy 47 0.699
574
PNC013 Pancreatic Ductal Carcinoma 48 0.699
575
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 28 0.699
576
GNT083 Genetic Neurodegenerative Disease 9 0.699
577
c SPR118 Spermatogenic Failure 1 36 0.680
578
RCK004 Rickets 65 0.680
579
INT395 Intracranial Meningioma 48 0.680
580
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.680
581
c 46X055 46,xy Sex Reversal 3 40 0.680
582
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.680
583
P DSR090 Disorder of Sexual Development 45 0.680
584
P FCL005 Focal Segmental Glomerulosclerosis 57 0.680
585
P THR014 Thrombocytopenia 66 0.680
586
MNN043 Meningioma, Familial 79 0.680
587
P SYS005 Systemic Scleroderma 73 0.680
588
RYN005 Raynaud Phenomenon 45 0.680
589
CLR030 Clear Cell Renal Cell Carcinoma 54 0.680
590
SCR001 Secretory Meningioma 40 0.680
591
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.680
592
P SYN140 Syndrome with 46,xy Disorder of Sex Development 23 0.680
593
GNT167 Genetic Obesity 32 0.680
594
P CLC063 Celiac Disease 1 66 0.660
595
P BRB001 Beriberi 44 0.660
596
P TBR001 Tuberous Sclerosis 69 0.660
597
c HRD010 Hereditary Spastic Paraplegia 65 0.660
598
P OLG002 Oligodendroglioma 66 0.660
599
P FML187 Familial Hypertension 34 0.660
600
SPC031 Specific Learning Disability 36 0.660
601
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.637
602
P FML340 Familial Episodic Pain Syndrome 50 0.637
603
c CHR711 Chronic Asthma 41 0.637
604
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.637
606
c SCH061 Schizophrenia 16 24 0.637
607
P INN002 Inner Ear Disease 50 0.637
608
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.637
609
HYP043 Hyperandrogenism 47 0.637
610
ANV001 Anovulation 46 0.637
611
P HYP076 Hyperthyroidism 53 0.637
612
P VTR007 Vitreoretinopathy 45 0.637
613
HLC007 Helicobacter Pylori Infection 67 0.612
614
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.612
615
FCL022 Focal Dystonia 41 0.612
616
DSC013 Discrimination, Two-Point, Reduction in 21 0.612
617
c BRD016 Bardet-Biedl Syndrome 4 44 0.612
618
c VRL010 Viral Hepatitis 52 0.612
619
c HPT003 Hepatitis a 63 0.612
620
c ADL052 Adult Acute Lymphocytic Leukemia 45 0.612
621
ENT004 Enthesopathy 51 0.612
622
P BRD002 Bardet-Biedl Syndrome 66 0.612
623
PLM010 Pulmonary Edema 54 0.612
624
DNT006 Dental Pulp Necrosis 43 0.612
625
P THY023 Thymoma 64 0.612
626
c THY107 Thymoma, Familial 42 0.612
627
CRB209 Cerebellar Malformation 22 0.612
628
P HYP265 Hypotonia 42 0.612
629
16P008 16p11.2 Duplication 16 0.612
630
DFN038 Dfnb1 34 0.612
631
CLP005 Ciliopathy 41 0.612
632
c VRL007 Viral Encephalitis 50 0.582
633
P NMN002 Niemann-Pick Disease 60 0.582
634
ATN004 Autonomic Neuropathy 42 0.582
635
P FBR017 Fibrosarcoma 55 0.582
636
c NMN015 Niemann-Pick Disease, Type C1 68 0.582
637
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.582
638
c MJR008 Major Affective Disorder 2 34 0.558
639
LGS001 Legius Syndrome 60 0.558
640
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.558
641
ANT039 Antisynthetase Syndrome 55 0.558
642
c FML001 Familial Atrial Fibrillation 65 0.558
643
c MJR004 Major Affective Disorder 4 28 0.558
644
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.558
645
c MJR023 Major Affective Disorder 7 33 0.558
646
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.558
647
NRN002 Neuronitis 31 0.558
648
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.558
649
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.558
650
P LKM062 Leukemia, Acute Lymphoblastic 69 0.551
651
LSC001 Lesch-Nyhan Syndrome 62 0.542
652
KBG001 Kbg Syndrome 54 0.542
653
CRN030 Coronary Stenosis 50 0.542
654
MLT157 Multiple System Atrophy 1 69 0.531
655
MLR004 Malaria 78 0.523
656
P CTR002 Cataract 59 0.496
657
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.477
658
IGR001 Ige Responsiveness, Atopic 59 0.468
659
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.468
660
P URT039 Urticaria 57 0.448
661
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.447
662
c DWL002 Dowling-Degos Disease 1 58 0.447
663
IDP031 Idiopathic Hypersomnia 39 0.447
664
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.447
665
c CHR087 Chronic Cystitis 37 0.427
666
P NSP012 Nasopharyngeal Carcinoma 60 0.427
667
P LYM118 Lymphoma 69 0.405
668
RTN017 Retinal Detachment 60 0.394
669
P FML011 Familial Adenomatous Polyposis 71 0.394
670
P ACN011 Acne 55 0.394
671
P HYP098 Hypereosinophilic Syndrome 66 0.394
672
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.382
673
P MCR010 Microcephaly 59 0.382
674
P GND004 Gonadal Dysgenesis 46 0.382
675
RDC002 Radiculopathy 51 0.382
676
c PRD040 Periodontitis, Chronic 52 0.370
677
P MLN007 Male Infertility 56 0.370
678
RHH001 Rohhad 27 0.370
679
CHC001 Chickenpox 56 0.370
680
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.357
681
ECT026 Ectopic Pregnancy 47 0.357
682
NNT008 Neonatal Abstinence Syndrome 40 0.357
683
MNT308 Mental Retardation with Optic Atrophy, Deafness, and Seizures 27 0.344
684
CHL065 Cholangiocarcinoma 58 0.344
685
INT079 Intrahepatic Cholangiocarcinoma 51 0.344
686
TXC005 Toxic Shock Syndrome 62 0.344
687
CRB090 Cerebral Hypoxia 42 0.344
688
SVR060 Severe X-Linked Intellectual Disability, Gustavson Type 24 0.344
689
CRH001 Crohn's Disease 80 0.344
690
SCR011 Scrapie 39 0.344
691
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.344
692
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.331
693
HRN029 Hearing Loss, Noise-Induced 37 0.331
694
P RSP003 Respiratory Failure 74 0.331
695
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.331
696
c LKM005 Leukemia, T-Cell, Chronic 33 0.331
697
LYM133 Lymphoma, Hodgkin, Classic 74 0.317
698
CRT013 Carotid Stenosis 51 0.317
699
P GCH001 Gaucher's Disease 69 0.317
700
WLL004 Wallerian Degeneration 38 0.317
701
KRT006 Keratoconjunctivitis 53 0.317
702
PST092 Posttransplant Acute Limbic Encephalitis 29 0.317
703
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.302
704
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.302
705
LMB062 Limb Ischemia 55 0.302
706
P ANG001 Angelman Syndrome 65 0.302
707
DTR001 Detrusor Sphincter Dyssynergia 37 0.302
708
ACQ007 Acquired Immunodeficiency Syndrome 58 0.302
709
LND001 Landau-Kleffner Syndrome 50 0.302
710
P KRN004 Kernicterus 47 0.302
711
OBS004 Obstructive Hydrocephalus 45 0.302
712
PRG001 Progressive Muscular Atrophy 41 0.302
713
ULC004 Ulcerative Colitis 74 0.302
714
NNT021 Neonatal Meningitis 22 0.302
715
P SCK005 Sickle Cell Disease 56 0.302
716
ATP013 Atopic Keratoconjunctivitis 41 0.302
717
ACT181 Acute Motor Axonal Neuropathy 25 0.302
718
P SRC025 Sarcoidosis 1 70 0.286
719
P ADL017 Adult T-Cell Leukemia 54 0.286
720
DFF005 Diffuse Large B-Cell Lymphoma 55 0.286
721
CHR710 Chronic Spontaneous Urticaria 45 0.286
722
c SCH045 Schizophrenia 12 23 0.286
723
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.286
724
TTT001 Tatton-Brown-Rahman Syndrome 45 0.286
725
ANT011 Antisocial Personality Disorder 47 0.286
726
SPN027 Spinal Stenosis 59 0.286
727
URM002 Uremia 47 0.286
728
P MLN008 Melanoma 75 0.286
729
P GLL022 Guillain-Barre Syndrome 59 0.286
730
PLM012 Pulmonary Sarcoidosis 53 0.286
731
P BNG032 Benign Mesothelioma 53 0.286
732
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.286
733
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.286
734
OTT002 Otitis Media 71 0.270
735
PHY008 Physical Urticaria 33 0.270
736
P HRS035 Hirschsprung Disease 1 66 0.270
737
MLT152 Multiple Self-Healing Squamous Epithelioma 45 0.270
738
CHL068 Cholestasis 61 0.270
739
CRV040 Cervix Carcinoma 50 0.270
740
CHR097 Chronic Purulent Otitis Media 34 0.270
741
SPP008 Suppurative Otitis Media 42 0.270
742
INT002 Intermittent Claudication 61 0.270
743
TRT001 Teratocarcinoma 41 0.270
744
P GLL018 Gallbladder Cancer 53 0.270
745
P ORT004 Orthostatic Intolerance 62 0.270
746
PHN003 Phenylketonuria 76 0.270
747
LNG030 Lung Adenoma 37 0.270
748
GNG004 Ganglioglioma 53 0.270
749
P ALP008 Alopecia 53 0.270
750
HYP034 Hypertensive Encephalopathy 43 0.270
751
P NRF002 Neurofibromatosis 60 0.270
752
ESP021 Esophageal Cancer 84 0.253
753
CYS001 Cystic Fibrosis 77 0.253
755
c DMN005 Diamond-Blackfan Anemia 2 28 0.253
756
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.253
757
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.253
758
ART165 Arthrogryposis Multiplex Congenita 3, Myogenic Type 31 0.253
759
P SJG008 Sjogren Syndrome 61 0.253
760
BLR001 Biliary Atresia 55 0.253
761
BRN002 Bronchiolitis 57 0.253
762
BRN024 Bronchitis 67 0.253
763
ACT049 Acute Disseminated Encephalomyelitis 53 0.253
764
RHM001 Rheumatic Fever 59 0.253
765
TTH006 Tooth Disease 51 0.253
766
INT066 Interstitial Lung Disease 60 0.253
767
CRT004 Carotid Artery Thrombosis 39 0.253
768
ADT003 Auditory System Disease 49 0.253
769
MCL006 Macular Retinal Edema 56 0.253
770
INT010 Intracranial Embolism 48 0.253
771
c LKM061 Leukemia, Acute Myeloid 83 0.253
772
DBT006 Diabetic Macular Edema 48 0.253
773
MNG007 Manganese Poisoning 28 0.253
774
URM005 Uremic Pruritus 45 0.253
775
GLC106 Glucocorticoid Resistance, Generalized 48 0.234
776
PMP014 Pemphigoid 49 0.234
777
P CTN015 Cutaneous T Cell Lymphoma 48 0.234
779
MTN003 Motion Sickness 50 0.234
780
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.234
781
MND023 Mend Syndrome 50 0.234
782
SRC014 Sarcoma 64 0.234
783
CNN001 Cannabis Dependence 38 0.234
784
LYM027 Lymphopenia 56 0.234
785
HYP026 Hypoglycemic Coma 37 0.234
786
PPL022 Papilloma 53 0.234
787
EXC002 Exocrine Pancreatic Insufficiency 42 0.234
788
SQM002 Squamous Cell Papilloma 45 0.234
789
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.234
790
c SCH085 Schizophrenia 2 27 0.234
791
SPN035 Spindle Cell Sarcoma 51 0.234
792
PTT037 Pituitary Tumors 44 0.234
793
BLL006 Bullous Pemphigoid 61 0.234
794
ADS004 Aids Dementia Complex 40 0.234
795
BSL008 Basal Ganglia Disease 41 0.234
796
P INF038 Influenza 68 0.234
797
P CHR071 Charcot-Marie-Tooth Disease 64 0.213
798
TNS005 Tonsillitis 57 0.213
799
APR001 Apraxia 51 0.213
800
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.213
801
CHD004 Chudley-Mccullough Syndrome 47 0.213
802
P HMN038 Human Coronavirus Sensitivity 30 0.213
803
c SCL052 Scleroderma, Familial Progressive 60 0.213
804
SNL009 Senile Plaque Formation 28 0.213
805
HND015 Hand Skill, Relative 29 0.213
806
IMP006 Impulse Control Disorder 45 0.213
807
ADL053 Adult Astrocytic Tumour 31 0.213
808
KRT002 Keratomalacia 54 0.213
809
SYN007 Synovitis 54 0.213
810
EPC002 Epicondylitis 43 0.213
811
PLC002 Plica Syndrome 35 0.213
812
CDQ001 Cauda Equina Syndrome 37 0.213
813
P CHR012 Chronic Granulomatous Disease 69 0.213
814
P ART021 Arteriosclerosis 53 0.213
815
PHR003 Pharyngitis 57 0.213
816
SPS019 Spastic Paraparesis 38 0.213
817
PRM003 Premature Ejaculation 44 0.213
818
ACT162 Acute Sensory Ataxic Neuropathy 24 0.213
819
PLM014 Pleomorphic Adenoma 51 0.213
820
WHP002 Whiplash 35 0.213
821
MLG079 Malignant Pleural Mesothelioma 42 0.213
822
P SPN237 Spina Bifida Aperta 19 0.213
823
c INH030 Inherited Retinal Disorder 28 0.213
824
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.213
825
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.191
826
BCT022 Bacterial Infectious Disease 56 0.191
827
P CRB045 Cerebellar Hypoplasia 40 0.191
828
P HYP111 Hyperprolinemia 44 0.191
829
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.191
830
ENT011 Enterocolitis 55 0.191
831
TNG009 Tongue Squamous Cell Carcinoma 43 0.191
832
P CND005 Cone Dystrophy 46 0.191
833
CHR174 Christianson Syndrome 47 0.191
834
OPP004 Oppositional Defiant Disorder 48 0.191
835
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 0.191
836
MYL057 Myelopathy, Htlv-1-Associated 39 0.191
837
CRD132 Cardiac Conduction Defect 59 0.191
838
SND001 Sandhoff Disease 66 0.191
839
HMF011 Hemifacial Spasm, Familial 33 0.191
840
c PST005 Posterior Uveitis 54 0.191
841
P TRN034 Transverse Myelitis 47 0.191
842
PRP027 Peripheral Vascular Disease 71 0.191
843
P MYP006 Myopia 55 0.191
844
P UVT001 Uveitis 57 0.191
845
P CCK001 Cockayne Syndrome 68 0.191
846
P DMY001 Demyelinating Polyneuropathy 41 0.191
847
c HPT001 Hepatitis C 61 0.191
848
QDR001 Quadriplegia 49 0.191
849
CRB033 Cerebral Degeneration 36 0.191
850
P NTR004 Neutropenia 62 0.191
851
CRN036 Craniopharyngioma 63 0.191
852
MMM001 Mammary Paget's Disease 53 0.191
853
PLG002 Plague 58 0.191
854
TRP002 Tropical Spastic Paraparesis 48 0.191
855
MYL001 Myelitis 49 0.191
856
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.191
857
GST010 Gestational Trophoblastic Neoplasm 52 0.191
858
CHM005 Chemical Colitis 33 0.191
859
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.191
860
OVR094 Ovarian Epithelial Cancer 39 0.191
861
P MYC033 Myoclonus 46 0.191
862
LNG099 Lung Disease 62 0.191
863
SCT002 Scotoma 42 0.191
864
CLL010 Cellular Ependymoma 58 0.191
865
P HMF004 Hemifacial Spasm 38 0.191
866
P MYT002 Myotonic Dystrophy 51 0.191
867
PRN019 Perinatal Necrotizing Enterocolitis 60 0.191
868
P GNG009 Gangliosidosis 44 0.191
869
GRN017 Granulocytopenia 42 0.191
870
CHR078 Chorioretinitis 50 0.191
871
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.191
872
ADG002 Audiogenic Seizures 25 0.191
873
P SKL032 Skeletal Muscle Disease 25 0.191
874
FCT007 Factor Vii Deficiency 64 0.165
875
MYC006 Mycosis Fungoides 65 0.165
876
PRX085 Preaxial Hallucal Polydactyly 28 0.165
877
DYS182 Dysphasia, Familial Developmental 34 0.165
878
P DNG005 Dengue Virus 55 0.165
879
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.165
880
DSS032 Disease by Infectious Agent 55 0.165
881
VTM002 Vitamin B12 Deficiency 48 0.165
882
P SPC019 Specific Language Impairment 31 0.165
883
P LYM033 Lymphoproliferative Syndrome 59 0.165
884
P FML023 Familial Hemiplegic Migraine 53 0.165
885
MYL020 Myelomeningocele 51 0.165
886
RSP021 Respiratory Allergy 41 0.165
887
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.165
888
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.165
889
c PRG020 Paragangliomas 3 39 0.165
890
P WSK001 Wiskott-Aldrich Syndrome 72 0.165
891
EWN003 Ewing Sarcoma 70 0.165
892
CRC014 Carcinoid Tumors, Intestinal 46 0.165
893
c DPH024 Diaphragmatic Hernia, Congenital 64 0.165
894
KRT019 Keratitis, Hereditary 66 0.165
895
WHM001 Whim Syndrome 60 0.165
896
WLL001 Williams-Beuren Syndrome 60 0.165
897
P HYP009 Hypertrophic Pyloric Stenosis 41 0.165
898
PYL006 Pyloric Stenosis 48 0.165
899
c ACT068 Acute Cystitis 61 0.165
900
IDP011 Idiopathic Interstitial Pneumonia 59 0.165
901
P LMY004 Leiomyosarcoma 62 0.165
902
P CRN025 Corneal Dystrophy 49 0.165
903
FST001 Foster-Kennedy Syndrome 39 0.165
904
URT001 Urethritis 52 0.165
905
FCH001 Fuchs' Endothelial Dystrophy 48 0.165
906
END011 Endometriosis of Ovary 40 0.165
907
P LVR013 Liver Disease 68 0.165
908
P LCT001 Lactic Acidosis 50 0.165
909
NNS002 Nonspecific Interstitial Pneumonia 42 0.165
910
P SKN015 Skin Carcinoma 71 0.165
911
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 48 0.165
912
UTR043 Uterine Sarcoma 40 0.165
913
DRG025 Drug-Induced Hearing Loss 22 0.165
914
TTR011 Tetraploidy 43 0.165
915
P PLY017 Polyarteritis Nodosa 60 0.165
916
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 38 0.165
917
P DYS005 Dyslexia 40 0.165
918
HYP264 Hypertonia 36 0.165
919
ATH004 Athetosis 25 0.165
920
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.165
921
NRT011 Neurotrophic Keratopathy 36 0.165
922
RSP018 Respiratory Bronchiolitis-Interstitial Lung Disease Syndrome 15 0.165
923
P ALP061 Alopecia, Androgenetic, 1 49 0.135
924
c CCK007 Cockayne Syndrome B 56 0.135
925
TRP006 Tarp Syndrome 58 0.135
926
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.135
927
P SPP010 Suppressor of Tumorigenicity 3 51 0.135
928
P MYS003 Myasthenia Gravis 68 0.135
929
TBL029 Tubulin, Beta 28 0.135
930
VLP002 Valproate Embryopathy 38 0.135
931
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.135
932
PYR010 Peyronie's Disease 50 0.135
933
RBF001 Riboflavin Deficiency 49 0.135
934
P KRT007 Keratoconus 50 0.135
935
OST003 Osteonecrosis 61 0.135
936
P KLF001 Kleefstra Syndrome 45 0.135
937
THY111 Thyroid Carcinoma, Familial Medullary 67 0.135
938
ACN002 Acanthosis Nigricans 56 0.135
939
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.135
940
c WLF013 Wolfram Syndrome 1 60 0.135
941
GLT035 Glutaric Acidemia I 57 0.135
942
P SCL018 Scoliosis 57 0.135
943
AND014 Androgenic Alopecia 46 0.135
944
P MYC084 Mycobacterium Tuberculosis 1 68 0.135
945
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 0.135
946
ANS021 Anisocoria 25 0.135
947
c MYP127 Myopia 2, Autosomal Dominant 26 0.135
948
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 61 0.135
949
IMM224 Immunodeficiency 68 36 0.135
950
LPT006 Leptin Receptor Deficiency 50 0.135
951
HSH003 Hashimoto Thyroiditis 60 0.135
952
DGR001 Digeorge Syndrome 62 0.135
953
ALP095 Alpha Thalassemia-X-Linked Intellectual Disability Syndrome 54 0.135
954
P PTS002 Ptosis 52 0.135
955
IGG001 Iga Glomerulonephritis 50 0.135
956